Hepalatide is under clinical development by Shanghai HEP Pharmaceutical and currently in Phase II for Hepatitis D. According to GlobalData, Phase II drugs for Hepatitis D have a 56% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Hepalatide’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Hepalatide overview
Synthetic Peptide (L-47) is under development for the treatment of hepatitis B and chronic hepatitis D. It is administered through subcutaneous route. The drug candidate is a synthetic peptide that acts by targeting sodium taurocholate co-transporting polypeptide (NTCP).
It was also under development for the treatment of type 2 diabetes.
For a complete picture of Hepalatide’s drug-specific PTSR and LoA scores, buy the report here.
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